Canonical Allele Identifier: CA1151518804
Gene: PLEKHG5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.6468551A= , CM000663.2:g.6468551A= GRCh38
NC_000001.10:g.6528611A= , CM000663.1:g.6528611A= GRCh37
NC_000001.9:g.6451198A= NCBI36
NG_007978.1:g.56459T= , LRG_262:g.56459T=
NG_029910.1:g.2645T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000340850.10:c.2285T= ENSP00000344570.5:p.Val762=
ENST00000377728.8:c.2285T= MANE Select ENSP00000366957.3:p.Val762=
ENST00000377740.5:c.2285T= ENSP00000366969.4:p.Val762=
ENST00000377748.6:c.2459T= ENSP00000366977.2:p.Val820=
ENST00000400913.6:c.2285T= ENSP00000383704.1:p.Val762=
ENST00000400915.8:c.2396T= ENSP00000383706.4:p.Val799=
ENST00000489097.6:n.2761T=
ENST00000535355.6:c.2492T= ENSP00000441445.1:p.Val831=
ENST00000537245.6:c.2396T= ENSP00000439625.2:p.Val799=
ENST00000673471.2:c.2582T= ENSP00000500749.1:p.Val861=
ENST00000674790.1:c.*2497T= ENSP00000502815.1:n.*2497T=
ENST00000675123.1:c.2249+491T= ENSP00000502132.1:n.2249+491T=
ENST00000675548.1:c.*2113T= ENSP00000502684.1:n.*2113T=
ENST00000675694.1:c.2285T= ENSP00000501925.1:p.Val762=
ENST00000675976.1:c.158T= ENSP00000501611.1:p.Val53=
ENST00000340850.9:c.2285T= ENSP00000344570.5:p.Val762=
ENST00000377725.5:c.2285T= ENSP00000366954.1:p.Val762=
ENST00000377728.7:c.2285T= ENSP00000366957.3:p.Val762=
ENST00000377732.5:c.2396T= ENSP00000366961.1:p.Val799=
ENST00000377740.4:c.2480+491T= ENSP00000366969.3:n.2480+491T=
ENST00000377748.5:c.2516T= ENSP00000366977.1:p.Val839=
ENST00000400913.5:c.2285T= ENSP00000383704.1:p.Val762=
ENST00000400915.7:c.2453T= ENSP00000383706.3:p.Val818=
ENST00000487949.4:n.1487T=
ENST00000489097.5:n.2761T=
ENST00000535355.5:c.2492T= ENSP00000441445.1:p.Val831=
ENST00000537245.5:c.2522T= ENSP00000439625.1:p.Val841=
NM_001042663.1:c.2453T= NP_001036128.1:p.Val818=
NM_001042664.1:c.2285T= NP_001036129.1:p.Val762=
NM_001042665.1:c.2285T= NP_001036130.1:p.Val762=
NM_001265592.1:c.2522T= NP_001252521.1:p.Val841=
NM_001265593.1:c.2492T= NP_001252522.1:p.Val831=
NM_001265594.1:c.2285T= NP_001252523.1:p.Val762=
NM_020631.4:c.2285T= NP_065682.2:p.Val762=
NM_198681.3:c.2516T= NP_941374.2:p.Val839=
NM_001042663.2:c.2453T= NP_001036128.1:p.Val818=
NM_001265594.2:c.2285T= NP_001252523.1:p.Val762=
NM_020631.5:c.2285T= NP_065682.2:p.Val762=
NM_001042663.3:c.2396T= NP_001036128.2:p.Val799=
NM_001265592.2:c.2396T= NP_001252521.2:p.Val799=
NM_020631.6:c.2285T= MANE Select NP_065682.2:p.Val762=
NM_198681.4:c.2285T= NP_941374.3:p.Val762=